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分子佐剂C3d3增强hCGβ蛋白疫苗免疫原性及其抗血清中和hCG生物学活性的作用
引用本文:王秀丽 李大金 袁敏敏 王明雁 朱影 孟毅. 分子佐剂C3d3增强hCGβ蛋白疫苗免疫原性及其抗血清中和hCG生物学活性的作用[J]. 实验生物学报, 2004, 37(4): 255-261
作者姓名:王秀丽 李大金 袁敏敏 王明雁 朱影 孟毅
摘    要:本文观察分子佐剂C3d3增强hCGβ蛋白避孕疫苗体液免疫效力的能力。采用分子生物学技术以phCMV1为载体分别构建分泌型、带有6个组氨酸纯化标签的真核表达质粒phCMV1-6His-hCGβ-C3d3和phCMV1-6His-hCGβ,在CHO细胞中获得重组蛋白的稳定、高效表达,并用镍柱和凝胶过滤层析对其进行分离、纯化。分别用hCGβ-C3d3融合蛋白、hCGβ 弗氏佐剂和单用hCGβ免疫生育期雌性BALB/c小鼠,共免疫两次,间隔4周。ELISA测定血清中抗hCGβ抗体滴度,并对各组小鼠产生的抗血清中和hCG生物学活性的能力进行比较。结果表明hCGβ单独免疫组在加强免疫后才见抗体生成,其抗体滴度比hCGβ-C3d3融合蛋白免疫组低1995倍,C3d3的佐剂能力是弗氏佐剂的10倍(初次免疫)-32倍(再次免疫),并且hCGβ-C3d3融合蛋白免疫小鼠产生的抗血清具有很强的中和hCG生物学活性的作用。实验证明通过分子佐剂C3d3可以大幅提高机体对hCGβ的体液免疫应答能力。

关 键 词:免疫避孕 分子佐剂 C3d3 hCGβ蛋白疫苗 避孕疫苗 抗血清

Enhancement of immunogenicity of hCGbeta protein vaccine and the hCG neutralization capacity of anti-serum by using the molecular adjuvant C3d3]
Xiu Li Wang,Da Jin Li,Min Min Yuan,Ming Yan Wang,Ying Zhu,Yi Meng. Enhancement of immunogenicity of hCGbeta protein vaccine and the hCG neutralization capacity of anti-serum by using the molecular adjuvant C3d3][J]. Acta Biologiae Experimentalis Sinica, 2004, 37(4): 255-261
Authors:Xiu Li Wang  Da Jin Li  Min Min Yuan  Ming Yan Wang  Ying Zhu  Yi Meng
Affiliation:Institute of Obstetrics and Gynecology, Fudan University, Shanghai 200011.
Abstract:To enhance the immunogenicity of hCGbeta protein vaccine and the hCG neutralization capacity of anti-serum by using the molecular adjuvant C3d3, the secreted 6his-hCGbeta-C3d3 fusion protein and 6his-hCGbeta were expressed in CHO cells and purified with Ni(2+)-chelating chromatography and Sephadex G-150 column. Then we investigated the potential of three copies of C3d as the molecular adjuvant of hCGbeta protein antigen. The antibody response to hCGbeta-C3d3 conjugates was compared with those resulting from immunization with hCGbeta alone and hCGbeta plus CFA/IFA in BALB/c mice. Our results showed that the antibody titer of hCGbeta-C3d3 was 1995-fold higher than that of hCGbeta alone and the anti-serum was capable effectively neutralizing the bioactivity of hCG. The immunity-enhancing action of C3d3 was 10-fold (primer) and 32-fold (booster) greater than CFA/IFA. These results indicated that C3d3 conjugates might be a better way to overcome the poor immunogenicity of hCGbeta contraceptive vaccine.
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